UNIVERSAL GENERATOR IRRIGATOR MODEL UGI-3000
K-Number: K884836 · 1988-12-06
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Device Summary
Frequently Asked Questions
What is the UNIVERSAL GENERATOR IRRIGATOR MODEL UGI-3000?
UNIVERSAL GENERATOR IRRIGATOR MODEL UGI-3000 is a medical device that received FDA 510(k) clearance on 1988-12-06. The listed applicant is Meditron Devices, Inc.. The 510(k) number is K884836.
When did UNIVERSAL GENERATOR IRRIGATOR MODEL UGI-3000 receive FDA 510(k) clearance?
UNIVERSAL GENERATOR IRRIGATOR MODEL UGI-3000 received FDA 510(k) clearance on 1988-12-06, under 510(k) number K884836.
Who is the listed applicant for UNIVERSAL GENERATOR IRRIGATOR MODEL UGI-3000?
The FDA 510(k) record lists Meditron Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNIVERSAL GENERATOR IRRIGATOR MODEL UGI-3000?
The FDA product code for UNIVERSAL GENERATOR IRRIGATOR MODEL UGI-3000 is GEI.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Meditron Devices, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: GEI)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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